A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671181



Internal ID9937286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15768791..15925975hg38UCSC Ensembl
Outerchr19:15768634..15926128hg38UCSC Ensembl
Innerchr19:15879601..16036785hg19UCSC Ensembl
Outerchr19:15879444..16036938hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38157495
hg19157495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5871097, essv5669872, essv6400688, essv5809399, essv6320364, essv6400246, essv5931669, essv5614343, essv6122058, essv6428287
SamplesNA18502, HG01052, HG01188, HG01198, HG00338, NA20535, HG00282, NA18537, HG00472, HG01061
Known GenesCYP4F11, CYP4F2, CYP4F24P, OR10H1, OR10H5, UCA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671181
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer